chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104888044548880446GC9GENIChomozygous116588646
104888044848880449C9GENIChomozygous128815377
104888046448880464C8GENIChomozygous128815378
104888049048880490G11GENIChomozygous128815379
104888049848880499G12GENIChomozygous128815380
104888050648880506C12GENIChomozygous128815381
104888051248880512G14GENIChomozygous128815382
104888054448880544C16GENIChomozygous128815383
104888055048880551A17GENIChomozygous128815384
104888055548880556C17GENIChomozygous128815385
104888055848880559T20GENIChomozygous128815386
104888056148880561GGGGGAAG20GENIChomozygous128815387
104888056548880566GA20GENIChomozygous118074756
104888057248880573TG20GENIChomozygous118036948
104888057548880575C19GENIChomozygous128815388
104888059348880593TTA21GENIChomozygous128815389
104888060048880600ATCTTT20GENIChomozygous128815390
104888060748880608CG22GENIChomozygous123355719
104888061048880610TC22GENIChomozygous128815391
104888062048880621A18GENIChomozygous128815392
104888062948880629T16GENIChomozygous128815393
104888074048880740T6GENIChomozygous128815399
104888075848880759TG9GENIChomozygous116977675
104888076748880767AG10GENIChomozygous128815400
104888076948880769G10GENIChomozygous128815401
104888077048880770GG11GENIChomozygous128815402
104888078248880782C12GENIChomozygous128815403
104888078748880787AT13GENIChomozygous128815404
104888079248880793AT13GENIChomozygous117218399
104888080348880803C13GENIChomozygous128815405
104888083248880832G13GENIChomozygous128815406
104888172048881721GT35GENICheterozygous118036951